chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77132609371326094AG28GENICpossibly homozygous53959347
77132714871327156GGCCTCAA--------32GENICpossibly homozygous54446616
77132784871327849AG21GENIChomozygous53959362
77132795571327956TA18GENIChomozygous53959366
77133008871330096TGTGTGTG--------2GENIChomozygous54981973
77133009771330098GC2GENIChomozygous54981975
77133010271330103A-2GENIChomozygous53959374
77133011071330111CG2GENIChomozygous54446620
77133011271330113CG3GENIChomozygous54446622
77133011971330120T-3GENIChomozygous54446624
77133012071330121GA3GENIChomozygous54981977
77133048171330482AT13GENIChomozygous54446626
77133060071330601AG20GENICpossibly homozygous53959376
77133080171330802CCTGTGTG5GENICheterozygous54981979
77133099271330993G-33GENICpossibly homozygous56336167
77133211971332120GA22GENIChomozygous54446628
77133300771333008CCATGA22GENIChomozygous53959378
77133406471334065AC22GENIChomozygous54446630
77133910871339114GTGAGA------20GENICpossibly homozygous54981981
77133912171339123AG--10GENICheterozygous54981985
77133972371339733ACACACACAC----------2GENICheterozygous54981987
77134058971340590G-26GENICpossibly homozygous54446636
77133003771330038AATCTCTCTC8GENIChomozygous54907019
77133937771339379TG--14GENIChomozygous54446632
77133951171339513TG--11GENIChomozygous54446634